| Dataset | ClinVar Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Oculocutaneous albinism type 7 (OCA7), formerly called OCA5, is a form of oculocutaneous albinism (OCA; see this term) characterized by skin and hair hypopigmentation, nystagmus and iris transillumination. (Orphanet Rare Disease Ontology, Orphanet_352745) |
| External Link | http://www.omim.org/entry/615179 |
| Similar Terms | |
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1 genes associated with the Oculocutaneous albinism type 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| C10ORF11 | chromosome 10 open reading frame 11 |
